A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6418



Internal ID15537446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:113996733..114042142hg38UCSC Ensembl
Outerchr10:115756492..115801901hg19UCSC Ensembl
Outerchr10:115746482..115791891hg18UCSC Ensembl
Outerchr10:115746482..115791891hg17UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg3845410
hg1945410
hg1845410
hg1745410
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7559
Supporting Variants
SamplesNA12156
Known Genes
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nssv6418
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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